نتایج جستجو برای: inhibitory concentration 50

تعداد نتایج: 882418  

Journal: :Antimicrobial agents and chemotherapy 1998
J J McSharry N S Lurain G L Drusano A L Landay M Notka M R O'Gorman A Weinberg H M Shapiro P S Reichelderfer C S Crumpacker

Rapid, quantitative, and objective determination of the susceptibilities of human cytomegalovirus (HCMV) clinical isolates to ganciclovir has been assessed by an assay that uses a fluorochrome-labeled monoclonal antibody to an HCMV immediate-early antigen and flow cytometry. Analysis of the ganciclovir susceptibilities of 25 phenotypically characterized clinical isolates by flow cytometry demon...

Journal: :South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2004
Milijaona Randrianarivelojosia Laurence Randrianasolo Rindra V Randremanana Arthur Randriamanantena Arsène Ratsimbasoa Jean-Désiré Rakotoson

OBJECTIVES To monitor the sensitivity of Plasmodium falciparum to the drugs used to treat severe malaria and to prevent malaria in Comoros and Madagascar. DESIGN We used the in vitro isotopic method to test the sensitivity of P. falciparum to quinine, mefloquine and cycloguanil. RESULTS We tested fresh isolates of P. falciparum, collected from patients living in urban, suburban and rural ar...

Journal: :Aquatic toxicology 2015
Mana M N Yung Stella W Y Wong Kevin W H Kwok F Z Liu Y H Leung W T Chan X Y Li A B Djurišić Kenneth M Y Leung

This study comprehensively investigated the influences of salinity, exposure concentration and time on the aggregate size, surface charge and dissolution of zinc oxide nanoparticles (ZnO-NPs; 20nm) in seawater, and examined the interacting effect of salinity and waterborne exposure of ZnO-NPs on the marine diatom Thalassiosira pseudonana for 96h. We found that aggregate sizes of ZnO-NPs signifi...

Journal: :European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V 2015
Jessica Soto Yucheng Sheng Joseph F Standing Mine Orlu Gul Catherine Tuleu

The rodent brief-access taste aversion (BATA) model is an efficient in vivo screening tool for taste assessment. A new E(max) (maximum effect attributable to the drug) model was developed and further investigated in comparison with three previously published models for analysing the rodent BATA data; the robustness of all the models was discussed. The rodent BATA data were obtained from a serie...

Journal: :Anais da Academia Brasileira de Ciencias 2017
Zenaide S Monte Amanda M Silva Gláucia M S Lima Teresinha G DA Silva Karla M R Marques Maria D Rodrigues Emerson P S Falcão Sebastião J Melo

A series of arylamidines 3a-j was designed, synthesized and investigated for antimicrobial activity. Structures of the compounds were confirmed by IR, 1H-NMR and 13C-NMR and a 2D spectroscopic study was performed. A preliminary screening of the antimicrobial tests clearly showed that three out of ten arylamidines, viz, 3f, 3g and 3i, were effective against all the gram-negative bacteria: Klebsi...

Journal: :Bulletin of the World Health Organization 1999
C Wongsrichanalai T Wimonwattrawatee P Sookto A Laoboonchai D G Heppner D E Kyle W H Wernsdorfer

Reported are the in vitro susceptibilities of Plasmodium falciparum to artesunate, mefloquine, quinine and chloroquine of 86 isolates and to dihydroartemisinin of 45 isolates collected from areas of high resistance to mefloquine within Thailand near the borders with Myanmar and Cambodia, and from southern Thailand where P. falciparum is generally still sensitive to mefloquine. All the isolates ...

Journal: :Journal of medicinal chemistry 1997
A S Tasker B K Sorensen H S Jae M Winn T W von Geldern D B Dixon W J Chiou B D Dayton S Calzadila L Hernandez K C Marsh J R WuWong T J Opgenorth

The benzodioxole ((methylenedioxy)benzene) group is present in a number of endothelin (ET) receptor antagonists thus far reported. As part of our own endothelin antagonist program we have developed (2R*,3R*,4S*)-1-(N,N-dibutylacetamido)-4-(1,3-benzodioxol-5- yl)-2-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid (A-127722). This is a potent antagonist, binding to the ETA and ETB receptor subtypes...

Journal: :Antimicrobial agents and chemotherapy 1995
H M Wardle D Law C B Moore C Mason D W Denning

We compared the in vitro activity of a new triazole, D0870, with those of fluconazole, itraconazole, and ketoconazole against 41 clinical isolates of fluconazole-resistant Candida belonging to nine different species. The 50% inhibitory concentrations (IC50s) were determined by a microdilution method with morpholinopropanesulfonic acid (MOPS)-buffered RPMI medium and an inoculum of approximately...

Journal: :Cancer research 1999
C Wandel R B Kim S Kajiji P Guengerich G R Wilkinson A J Wood

Many P-glycoprotein (P-gp) inhibitors studied in vitro and in vivo are also known or suspected to be substrates and/or inhibitors of cytochrome P-450 3A (CYP3A). Such overlap raises the question of whether CYP3A inhibition is an intrinsic characteristic of P-gp inhibitors, a matter of concern in the development and rational use of such agents. Thus, the purpose of the present study was to deter...

2013
Hui Zhang Jeanne Holden-Wiltse Jiong Wang Hua Liang

The half-maximal inhibitory concentration IC[Formula: see text] is an important pharmacodynamic index of drug effectiveness. To estimate this value, the dose response relationship needs to be established, which is generally achieved by fitting monotonic sigmoidal models. However, recent studies on Human Immunodeficiency Virus (HIV) mutants developing resistance to antiviral drugs show that the ...

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